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206 related items for PubMed ID: 25449630

  • 1. Germline PRKACA amplification leads to Cushing syndrome caused by 3 adrenocortical pathologic phenotypes.
    Carney JA, Lyssikatos C, Lodish MB, Stratakis CA.
    Hum Pathol; 2015 Jan; 46(1):40-9. PubMed ID: 25449630
    [Abstract] [Full Text] [Related]

  • 2. Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations.
    Lodish MB, Yuan B, Levy I, Braunstein GD, Lyssikatos C, Salpea P, Szarek E, Karageorgiadis AS, Belyavskaya E, Raygada M, Faucz FR, Izzat L, Brain C, Gardner J, Quezado M, Carney JA, Lupski JR, Stratakis CA.
    Eur J Endocrinol; 2015 Jun; 172(6):803-11. PubMed ID: 25924874
    [Abstract] [Full Text] [Related]

  • 3. PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases.
    Thiel A, Reis AC, Haase M, Goh G, Schott M, Willenberg HS, Scholl UI.
    Eur J Endocrinol; 2015 Jun; 172(6):677-85. PubMed ID: 25750087
    [Abstract] [Full Text] [Related]

  • 4. Primary pigmented nodular adrenocortical disease: the original 4 cases revisited after 30 years for follow-up, new investigations, and molecular genetic findings.
    Carney JA, Libé R, Bertherat J, Young WF.
    Am J Surg Pathol; 2014 Sep; 38(9):1266-73. PubMed ID: 24805858
    [Abstract] [Full Text] [Related]

  • 5. Familial micronodular adrenocortical disease, Cushing syndrome, and mutations of the gene encoding phosphodiesterase 11A4 (PDE11A).
    Carney JA, Gaillard RC, Bertherat J, Stratakis CA.
    Am J Surg Pathol; 2010 Apr; 34(4):547-55. PubMed ID: 20351491
    [Abstract] [Full Text] [Related]

  • 6. Somatic PRKACA Mutations: Association With Transition From Pituitary-Dependent to Adrenal-Dependent Cushing Syndrome.
    Di Dalmazi G, Timmers HJLM, Arnaldi G, Küsters B, Scarpelli M, Bathon K, Calebiro D, Beuschlein F, Hermus A, Reincke M.
    J Clin Endocrinol Metab; 2019 Nov 01; 104(11):5651-5657. PubMed ID: 31276155
    [Abstract] [Full Text] [Related]

  • 7. Cushing's syndrome due to ACTH-independent bilateral adrenocortical macronodular hyperplasia.
    Terzolo M, Boccuzzi A, Ali A, Bollito E, De Risi C, Paccotti P, Angeli A.
    J Endocrinol Invest; 1997 May 01; 20(5):270-5. PubMed ID: 9258806
    [Abstract] [Full Text] [Related]

  • 8. Germline PRKACA amplification-associated primary pigmented nodular adrenocortical disease: a case report and literature review.
    Yang WR, Liang XH, Qin YF, Yang HY, He SZ, Huang ZX, Liu YP, Luo ZJ.
    Arch Endocrinol Metab; 2023 Nov 17; 68():e220491. PubMed ID: 37988664
    [Abstract] [Full Text] [Related]

  • 9. Protein kinase A defects and cortisol-producing adrenal tumors.
    Zilbermint M, Stratakis CA.
    Curr Opin Endocrinol Diabetes Obes; 2015 Jun 17; 22(3):157-62. PubMed ID: 25871963
    [Abstract] [Full Text] [Related]

  • 10. PRKAR1A-negative familial Cushing's syndrome: two case reports.
    Lim LL, Kitan N, Paramasivam SS, Ratnasingam J, Ibrahim L, Chan SP, Tan AT, Vethakkan SR.
    J Med Case Rep; 2015 Dec 01; 9():277. PubMed ID: 26619967
    [Abstract] [Full Text] [Related]

  • 11. Cushing's syndrome due to primary pigmented nodular adrenocortical disease--a case report reviews of the literature.
    Choi KM, Seu JH, Kim YH, Lee EJ, Kim SJ, Baik SH, Choi DS.
    Korean J Intern Med; 1995 Jan 01; 10(1):68-72. PubMed ID: 7626560
    [Abstract] [Full Text] [Related]

  • 12. Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia.
    Storr HL, Mitchell H, Swords FM, Main KM, Hindmarsh PC, Betts PR, Shaw NJ, Johnston DI, Clark AJ, Reznek RH, Grossman AB, Savage MO.
    Clin Endocrinol (Oxf); 2004 Nov 01; 61(5):553-9. PubMed ID: 15521956
    [Abstract] [Full Text] [Related]

  • 13. Bilateral primary pigmented nodular adrenocortical disease. Rare cause of the Cushing syndrome.
    Shenoy BV, Carpenter PC, Carney JA.
    Am J Surg Pathol; 1984 May 01; 8(5):335-44. PubMed ID: 6329005
    [Abstract] [Full Text] [Related]

  • 14. Rebound thymic hyperplasia after adrenalectomy in a patient with Cushing syndrome caused by adrenocortical adenoma: A case report.
    Hwang JW, Hwang PH.
    Medicine (Baltimore); 2018 Apr 01; 97(15):e0367. PubMed ID: 29642186
    [Abstract] [Full Text] [Related]

  • 15. Acromegaly with hyperprolactinemia developed after bilateral adrenalectomy in a patient with Cushing's syndrome due to adrenocortical nodular hyperplasia.
    Ogo A, Haji M, Natori S, Kanzaki T, Kabayama Y, Osamura RY, Nawata H, Ibayashi H.
    Endocr J; 1993 Feb 01; 40(1):17-25. PubMed ID: 7951491
    [Abstract] [Full Text] [Related]

  • 16. Cushing's syndrome due to unilateral adrenocortical hyperplasia.
    Otsuka F, Ogura T, Nakao K, Hayakawa N, Mimura Y, Yamauchi T, Makino H.
    Intern Med; 1998 Apr 01; 37(4):385-90. PubMed ID: 9630199
    [Abstract] [Full Text] [Related]

  • 17. Primary bimorphic adrenocortical disease: cause of hypercortisolism in McCune-Albright syndrome.
    Carney JA, Young WF, Stratakis CA.
    Am J Surg Pathol; 2011 Sep 01; 35(9):1311-26. PubMed ID: 21836496
    [Abstract] [Full Text] [Related]

  • 18. Cushing´s syndrome due to bilateral adrenal cortical disease: Bilateral macronodular adrenal cortical disease and bilateral micronodular adrenal cortical disease.
    Araujo-Castro M, Marazuela M.
    Front Endocrinol (Lausanne); 2022 Sep 01; 13():913253. PubMed ID: 35992106
    [Abstract] [Full Text] [Related]

  • 19. Long-Term Outcome of Primary Bilateral Macronodular Adrenocortical Hyperplasia After Unilateral Adrenalectomy.
    Osswald A, Quinkler M, Di Dalmazi G, Deutschbein T, Rubinstein G, Ritzel K, Zopp S, Bertherat J, Beuschlein F, Reincke M.
    J Clin Endocrinol Metab; 2019 Jul 01; 104(7):2985-2993. PubMed ID: 30844071
    [Abstract] [Full Text] [Related]

  • 20. [Morphology of the adrenal cortex in Cushing's syndrome].
    Flattet A, Hedinger C.
    Schweiz Med Wochenschr; 1980 Sep 06; 110(36):1300-6. PubMed ID: 7444415
    [Abstract] [Full Text] [Related]

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